BDBM50119733 CHEMBL102840::N-{(S)-1-[3-(4-Acetyl-phenoxy)-propyl]-pyrrolidin-3-yl}-4-cyano-benzenesulfonamide

SMILES CC(=O)c1ccc(OCCCN2CC[C@@H](C2)NS(=O)(=O)c2ccc(cc2)C#N)cc1

InChI Key InChIKey=DIEXZKWJXAPYGJ-FQEVSTJZSA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50119733   

TargetHistamine H3 receptor(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50119733(CHEMBL102840 | N-{(S)-1-[3-(4-Acetyl-phenoxy)-prop...)
Affinity DataKi:  6nMAssay Description:Binding affinity against rat histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H2 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50119733(CHEMBL102840 | N-{(S)-1-[3-(4-Acetyl-phenoxy)-prop...)
Affinity DataKi:  2.30E+3nMAssay Description:Binding affinity to the human Histamine H2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50119733(CHEMBL102840 | N-{(S)-1-[3-(4-Acetyl-phenoxy)-prop...)
Affinity DataKi:  1.40E+4nMAssay Description:Binding affinity to the human Histamine H1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed